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Canadian Journal of Cardiology, 2020
BACKGROUND Brugada syndrome is a major cause of sudden cardiac death in young people with a distinctive electrocardiogram (ECG) feature. We aimed to develop a deep learning-enabled ECG model for automatic screening Brugada syndrome to identify these ...
Chih-Min Liu +17 more
semanticscholar +1 more source
BACKGROUND Brugada syndrome is a major cause of sudden cardiac death in young people with a distinctive electrocardiogram (ECG) feature. We aimed to develop a deep learning-enabled ECG model for automatic screening Brugada syndrome to identify these ...
Chih-Min Liu +17 more
semanticscholar +1 more source
Brugada syndrome and syncope: a practical approach for diagnosis and treatment.
Europace, 2020Syncope in patients with Brugada electrocardiogram pattern may represent a conundrum in the decision algorithm because incidental benign forms, especially neurally mediated syncope, are very frequent in this syndrome similarly to the general population ...
G. Mascia +7 more
semanticscholar +1 more source
Brugada syndrome and syncope: A systematic review
Cardiovascular Electrophysiology, 2020Distinguishing syncope due to malignant arrhythmias from an incidental benign form in Brugada syndrome (BrS) is often difficult. Through systematic literature review, we evaluated the role of syncope in predicting subsequent malignant arrhythmias in BrS.
G. Mascia +5 more
semanticscholar +1 more source
Acta Cardiologica, 2009
The Brugada syndrome is an inherited cardiac disorder initially described in 1992 by Pedro and Josep Brugada, with variable electrocardiographic features characteristic of right bundle-branch block, persistent ST-segment elevation in the precordial leads (VI-V3) at rest and sudden cardiac death.
Mario Jiménez-Hernández +4 more
openaire +3 more sources
The Brugada syndrome is an inherited cardiac disorder initially described in 1992 by Pedro and Josep Brugada, with variable electrocardiographic features characteristic of right bundle-branch block, persistent ST-segment elevation in the precordial leads (VI-V3) at rest and sudden cardiac death.
Mario Jiménez-Hernández +4 more
openaire +3 more sources
Cardiac Electrophysiology Clinics, 2016
Brugada syndrome might stay undetected in patients until surviving cardiac arrest. Despite the prominent advances in exploring the disease in the past 2 decades, many questions remain unanswered and the controversies continue. Despite all mutations identified to be associated with the disease, two-thirds of cases have a negative genetic test.
Marwan M, Refaat +2 more
openaire +3 more sources
Brugada syndrome might stay undetected in patients until surviving cardiac arrest. Despite the prominent advances in exploring the disease in the past 2 decades, many questions remain unanswered and the controversies continue. Despite all mutations identified to be associated with the disease, two-thirds of cases have a negative genetic test.
Marwan M, Refaat +2 more
openaire +3 more sources
Atrial fibrillation in Brugada syndrome: Current perspectives
Cardiovascular Electrophysiology, 2020The incidence of atrial fibrillation (AF) in Brugada syndrome (BrS) has been reported at between 9% and 53% by different series, but the true prevalence is unknown. However, AF may be the presenting feature in some patients. The underlying mechanisms for
K. Vlachos +16 more
semanticscholar +1 more source
Current Opinion in Cardiology, 2002
The Brugada syndrome describes a subgroup of patients at risk for the occurrence of ventricular fibrillation who have no definable structural heart disease associated with a right bundle branch block conduction pattern and ST-segment elevation in the right precordial leads.
Gerald V, Naccarelli +3 more
openaire +2 more sources
The Brugada syndrome describes a subgroup of patients at risk for the occurrence of ventricular fibrillation who have no definable structural heart disease associated with a right bundle branch block conduction pattern and ST-segment elevation in the right precordial leads.
Gerald V, Naccarelli +3 more
openaire +2 more sources
Worldwide Prevalence of Brugada Syndrome: A Systematic Review and Meta-Analysis.
Acta Cardiologica Sinica, 2018Background Brugada syndrome (BrS) is considered to be an inherited arrhythmic disease associated with fatal complications and premature sudden unexpected death.
W. Vutthikraivit +6 more
semanticscholar +1 more source
Cardiology in Review, 1999
In 1992, Brugada and Brugada reported a distinct subgroup of patients with episodes of "idiopathic"polymorphic ventricular tachycardia or ventricular fibrillation characterized by a unique electrocardiographic (ECG) pattern, which consisted of right bundle branch block and ST-segment elevation from V1 to V2-V3. As in patients with long QT syndrome, the
CORRADO, DOMENICO +4 more
openaire +4 more sources
In 1992, Brugada and Brugada reported a distinct subgroup of patients with episodes of "idiopathic"polymorphic ventricular tachycardia or ventricular fibrillation characterized by a unique electrocardiographic (ECG) pattern, which consisted of right bundle branch block and ST-segment elevation from V1 to V2-V3. As in patients with long QT syndrome, the
CORRADO, DOMENICO +4 more
openaire +4 more sources
Current Opinion in Cardiology, 2010
The Brugada syndrome has been investigated in depth since its description in 1992 both on a clinical and on a basic research level. Since the discovery of the first genetic defect in 1998, several genes have been subsequently identified. However, to date all these genes together explain only 30% of the cases, indicating that there is still an important
Anna Iglesias +2 more
openaire +3 more sources
The Brugada syndrome has been investigated in depth since its description in 1992 both on a clinical and on a basic research level. Since the discovery of the first genetic defect in 1998, several genes have been subsequently identified. However, to date all these genes together explain only 30% of the cases, indicating that there is still an important
Anna Iglesias +2 more
openaire +3 more sources